16 research outputs found

    Habitudes Alimentaires au Niger : Cartographie des Recettes Culinaires des MĂ©nages

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    Depuis la crise de 2005, les taux de personnes atteints de sous-nutrition Ă©voluent en dents de scie au Niger, d’oĂč la stratĂ©gie de l’état d’amĂ©liorer l’alimentation des populations pour y remĂ©dier.  La prĂ©sente Ă©tude vise Ă  Ă©tablir, toutes les recettes alimentaires, leurs ingrĂ©dients et les aliments communĂ©ment consommĂ©s dans les mĂ©nages au Niger. Ces derniers ont Ă©tĂ© collectĂ©s auprĂšs de plusieurs sources, rĂ©organisĂ©es dans une base de donnĂ©es suivant l’écriture du standard international « INFOODS Â». C’est ainsi, qu’un total de 518 recettes alimentaires a Ă©tĂ© rĂ©pertoriĂ© dont 269 recettes Ă  base de cĂ©rĂ©ales, 36 de tubercules, 33 de lĂ©gumineuses, 15 pour les produits carnĂ©s, 3 Ă  base de laits et produits laitiers, 100 recettes de lĂ©gumes, 26 de lĂ©gumes feuilles pour les sauces, 31 recettes Ă  base de fruits, 1 Ă  base de noix et graines et 4 recettes Ă  base d’Ɠufs. Les plus reprĂ©sentĂ©es sont celles de bouillies de cĂ©rĂ©ales et mĂ©langes(145), et salades de lĂ©gumes (82) suivies des boules (27) et couscous de cĂ©rĂ©ales(26), sauces(26), purĂ©es de lĂ©gumes (25) et enfin les pates de cĂ©rĂ©ales(16), ragouts de tubercules(11), jus de fruits (14), cĂ©rĂ©ales cuites (7), pates de tubercules (5), beignets de cĂ©rĂ©ales(5), jus de lĂ©gumes(5), galettes de cĂ©rĂ©ales (6), couscous de lĂ©gumineuses (6), farines (5), fritures de tubercules,(5), grillades de produits carnĂ©s(8), biscuits de lĂ©gumineuses (6), et les gĂąteaux de cĂ©rĂ©ales (7). Cette copulation des recettes constitue Ă  travers l’élaboration d’un dictionnaire de code de recettes alimentaires et aliments, le point de dĂ©part de la premiĂšre Ă©tape de l’étude de consommation alimentaire des groupes vulnĂ©rables au Niger.   Since the 2005 crisis, the rates of people suffering from undernutrition have been on the rise in Niger, hence the state strategy to improve the diet of the population to remedy this. This study aims to establish all the food recipes, their ingredients and the foods commonly consumed in households in Niger. These were collected from several sources, reorganized in a database following the writing of the international standard « INFOODS Â». Thus, a total of 518 food recipes have been listed including 269 recipes based on cereals, 36 on tubers, 33 on legumes, 15 for meat products, 3 based on milk and dairy products, 100 recipes for vegetables, 26 leafy greens for sauces, 31 fruit-based recipes, 1 nut and seed-based and 4 egg-based recipes. The most represented are those of cereal porridges and mixtures (145), and vegetable salads (82) followed by balls (27) and cereal couscous (26), sauces (26), vegetable purees (25) and finally cereal pasta(16), tuber ragout(11), fruit juice(14), cooked cereal(7), tuber pasta(5), cereal fritters(5), vegetable juice(5), cereals (6), legume couscous (6), flour (5), fried tubers (5), grilled meat products (8), legume biscuits (6), and cereal cakes (7) . This copulation of recipes constitutes, through the development of a code dictionary of food recipes and foods, the starting point of the first stage of the food consumption study of vulnerable groups in Niger

    Prevalence of Mutations in the \u3ci\u3ePfdhfr\u3c/i\u3e, \u3ci\u3ePfdhps\u3c/i\u3e, and \u3ci\u3ePfmdr1\u3c/i\u3e Genes of Malarial Parasites Isolated from Symptomatic Patients in Dogondoutchi, Niger

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    The effectiveness of artemisinin-based combination therapies (ACTs) depends not only on that of artemisinin but also on that of partner molecules. This study aims to evaluate the prevalence of mutations in the Pfdhfr, Pfdhps, and Pfmdr1 genes from isolates collected during a clinical study. Plasmodium genomic DNA samples extracted from symptomatic malaria patients from Dogondoutchi, Niger, were sequenced by the Sanger method to determine mutations in the Pfdhfr (codons 51, 59, 108, and 164), Pfdhps (codons 436, 437, 540, 581, and 613), and Pfmdr1 (codons 86, 184, 1034, and 1246) genes. One hundred fifty-five (155) pre-treatment samples were sequenced for the Pfdhfr, Pfdhps, and Pfmdr1 genes. A high prevalence of mutations in the Pfdhfr gene was observed at the level of the N51I (84.97%), C59R (92.62%), and S108N (97.39%) codons. The key K540E mutation in the Pfdhps gene was not observed. Only one isolate was found to harbor a mutation at codon I431V. The most common mutation on the Pfmdr1 gene was Y184F in 71.43% of the mutations found, followed by N86Y in 10.20%. The triple-mutant haplotype N51I/C59R/S108N (IRN) was detected in 97% of the samples. Single-mutant (ICS and NCN) and double-mutant (IRS, NRN, and ICN) haplotypes were prevalent at 97% and 95%, respectively. Double-mutant haplotypes of the Pfdhps (581 and 613) and Pfmdr (86 and 184) were found in 3% and 25.45% of the isolates studied, respectively. The study focused on the molecular analysis of the sequencing of the Pfdhfr, Pfdhps, and Pfmdr1 genes. Although a high prevalence of mutations in the Pfdhfr gene have been observed, there is a lack of sulfadoxine pyrimethamine resistance. There is a high prevalence of mutation in the Pfmdr184 codon associated with resistance to amodiaquine. These data will be used by Niger’s National Malaria Control Program to better monitor the resistance of Plasmodium to partner molecules in artemisinin-based combination therapies

    A refined estimate of the malaria burden in Niger

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    <p>Abstract</p> <p>Background</p> <p>The health authorities of Niger have implemented several malaria prevention and control programmes in recent years. These interventions broadly follow WHO guidelines and international recommendations and are based on interventions that have proved successful in other parts of Africa. Most performance indicators are satisfactory but, paradoxically, despite the mobilization of considerable human and financial resources, the malaria-fighting programme in Niger seems to have stalled, as it has not yet yielded the expected significant decrease in malaria burden. Indeed, the number of malaria cases reported by the National Health Information System has actually increased by a factor of five over the last decade, from about 600,000 in 2000 to about 3,000,000 in 2010. One of the weaknesses of the national reporting system is that the recording of malaria cases is still based on a presumptive diagnosis approach, which overestimates malaria incidence.</p> <p>Methods</p> <p>An extensive nationwide survey was carried out to determine by microscopy and RDT testing, the proportion of febrile patients consulting at health facilities for suspected malaria actually suffering from the disease, as a means of assessing the magnitude of this problem and obtaining a better estimate of malaria morbidity in Niger.</p> <p>Results</p> <p>In total, 12,576 febrile patients were included in this study; 57% of the slides analysed were positive for the malaria parasite during the rainy season, when transmission rates are high, and 9% of the slides analysed were positive during the dry season, when transmission rates are lower. The replacement of microscopy methods by rapid diagnostic tests resulted in an even lower rate of confirmation, with only 42% of cases testing positive during the rainy season, and 4% during the dry season. Fever alone has a low predictive value, with a low specificity and sensitivity. These data highlight the absolute necessity of confirming all reported malaria cases by biological diagnosis methods, to increase the accuracy of the malaria indicators used in monitoring and evaluation processes and to improve patient care in the more remote areas of Niger. This country extends over a large range of latitudes, resulting in the existence of three major bioclimatic zones determining vector distribution and endemicity.</p> <p>Conclusion</p> <p>This survey showed that the number of cases of presumed malaria reported in health centres in Niger is largely overestimated. The results highlight inadequacies in the description of the malaria situation and disease risk in Niger, due to the over-diagnosis of malaria in patients with simple febrile illness. They point out the necessity of confirming all cases of suspected malaria by biological diagnosis methods and the need to take geographic constraints into account more effectively, to improve malaria control and to adapt the choice of diagnostic method to the epidemiological situation in the area concerned. Case confirmation will thus also require a change in behaviour, through the training of healthcare staff, the introduction of quality control, greater supervision of the integrated health centres, the implementation of good clinical practice and a general optimization of the use of available diagnostic methods.</p

    Treatment outcomes and associated factors for hospitalization of children treated for acute malnutrition under the OptiMA simplified protocol: a prospective observational cohort in rural Niger

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    IntroductionGlobally, access to treatment for severe and moderate acute malnutrition is very low, in part because different protocols and products are used in separate programs. New approaches, defining acute malnutrition (AM) as mid-upper arm circumference (MUAC) &lt; 125 mm or oedema, are being investigated to compare effectiveness to current programs. Optimizing Malnutrition treatment (OptiMA) is one such strategy that treats AM with one product – ready-to-use therapeutic food, or RUTF – at reduced dosage as the child improves.MethodsThis study aimed to determine whether OptiMA achieved effectiveness benchmarks established in the Nigerien National Nutrition protocol. A prospective cohort study of children in the rural Mirriah district evaluated outcomes among children 6-59 months with uncomplicated AM treated under OptiMA. In a parallel, unconnected program in one of the two trial sites, all non-malnourished children 6-23 months of age were provided small quantity lipid-based nutritional supplements (SQ-LNS). A multivariate logistic regression identified factors associated with hospitalization.ResultsFrom July-December 2019, 1,105 children were included for analysis. Prior to treatment, 39.3% of children received SQ-LNS. Recovery, non-response, and mortality rates were 82.3%, 12.6%, and 0.7%, respectively, and the hospitalization rate was 15.1%. Children who received SQ-LNS before an episode of AM were 43% less likely to be hospitalized (ORa=0.57; 0.39-0.85, p = 0.004).DiscussionOptiMA had acceptable recovery compared to the Nigerien reference but non-response was high. Children who received SQ-LNS before treatment under OptiMA were less likely to be hospitalized, showing potential health benefits of combining simplified treatment protocols with food-based prevention in an area with a high burden of malnutrition such as rural Niger

    Long-term cellular immunity of vaccines for Zaire Ebola Virus Diseases

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    Recent Ebola outbreaks underscore the importance of continuous prevention and disease control efforts. Authorized vaccines include Merck’s Ervebo (rVSV-ZEBOV) and Johnson & Johnson’s two-dose combination (Ad26.ZEBOV/MVA-BN-Filo). Here, in a five-year follow-up of the PREVAC randomized trial (NCT02876328), we report the results of the immunology ancillary study of the trial. The primary endpoint is to evaluate long-term memory T-cell responses induced by three vaccine regimens: Ad26–MVA, rVSV, and rVSV–booster. Polyfunctional EBOV-specific CD4+ T-cell responses increase after Ad26 priming and are further boosted by MVA, whereas minimal responses are observed in the rVSV groups, declining after one year. In-vitro expansion for eight days show sustained EBOV-specific T-cell responses for up to 60 months post-prime vaccination with both Ad26-MVA and rVSV, with no decline. Cytokine production analysis identify shared biomarkers between the Ad26-MVA and rVSV groups. In secondary endpoint, we observed an elevation of pro-inflammatory cytokines at Day 7 in the rVSV group. Finally, we establish a correlation between EBOV-specific T-cell responses and anti-EBOV IgG responses. Our findings can guide booster vaccination recommendations and help identify populations likely to benefit from revaccination

    C50 - Evaluation de l’utilisation de la liste nationale des mĂ©dicaments essentiels au Mali

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    Introduction : La liste nationale des mĂ©dicaments essentiels (LNME), version de 2019, est un outil privilĂ©giĂ© pour la mise en Ɠuvre de la politique pharmaceutique nationale (PPN) au Mali. Elle participe Ă  la rationalisation de la prescription. Elle est mise Ă  jour tous les 2 ans. L’objectif Ă©tait d’évaluer l’utilisation de la LNME par les prestataires avant sa rĂ©vision. MĂ©thodologie : Il s’agissait d’une Ă©tude transversale, rĂ©alisĂ©e du 1er fĂ©vrier au 31 mars 2023 dans les structures sanitaires. La taille de l’échantillon a Ă©tĂ© dĂ©terminĂ©e par la formule de Schwartz qui a permis de sĂ©lectionner en fonction de leurs poids les rĂ©gions de Sikasso, SĂ©gou et le district de Bamako. Les donnĂ©es ont Ă©tĂ© collectĂ©es avec l’application KoboCollect. Les logiciels ExcelÂź-2019 et SPSSÂź-22.0 ont servi Ă  l’analyse des donnĂ©es. RĂ©sultats : Au total 457 agents de santĂ© ont Ă©tĂ© enquĂȘtĂ©s dont 380 prescripteurs et 77 gestionnaires de mĂ©dicaments dans 61 structures visitĂ©es. La LNME Ă©tait disponible dans 49% des structures. Environ 65% des gestionnaires et 6% des prescripteurs disposaient de la LNME. En somme, 50% des gestionnaires et 3% des prescripteurs l’utilisaient rĂ©guliĂšrement pour l’approvisionnement en mĂ©dicaments et la prescription. Les raisons de la faible utilisation de la LNME Ă©taient diverses. Le dĂ©lai moyen entre la rĂ©vision de la LNME 2019 et la rĂ©ception par les structures Ă©tait de 1,8 an. Sur une liste de 30 mĂ©dicaments Ă©valuĂ©s, la disponibilitĂ© moyenne le jour de la visitĂ© Ă©tait de 19,75%. Par ailleurs, 27% des prescripteurs et 87% des gestionnaires inclus avaient respectivement reçu une formation en prescription rationnelle et en gestion logistique. Conclusion : La mise Ă  disposition rapide de la LNME et la disponibilitĂ© continue de tous les mĂ©dicaments y figurant pourrait renforcer son appropriation et son utilisation par les acteur

    Life-threatening malaria in African children a prospective study in a mesoendemic urban setting

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    International audienceBACKGROUND:The population exposed to malaria within African cities has steadily increased. However, comprehensive data on life-threatening malaria features and risk factors in children from urban areas with seasonal malaria transmission, such as in Bamako (Mali), are lacking.METHODS:Children admitted to the Gabriel Touré Hospital in Bamako with severe malarial anemia (SMA) and/or cerebral malaria (CM) were prospectively included in the study. Indicators of either SMA or CM were analyzed using logistic regression; and death hazard ratios (HRs) were estimated through survival analysis.RESULTS:The study included 455 children: 66% presented with CM, 34% with SMA, 3% with hypoglycemia (HG); 5% with dehydration; 17% with respiratory distress (RD); 25% with splenomegaly; and 92% with hepatomegaly. The children with CM were older than those with SMA. CM was more often associated with dehydration, HG, and RD, whereas SMA was more often associated with splenomegaly. The overall case fatality rate was 16%, and 94% of the children who died had CM. HG [HR: 2.37; 95% confidence interval (CI): 1.04-5.39; P = 0.040], RD (HR: 4.23; 95% CI: 2.46-7.30; P < 10(-6)) and a deep coma with a Blantyre score of less than 3 (HR: 6.78, 95% CI: 2.43-18.91; P < 10(-3)), were all independent predictors of death.CONCLUSIONS:These findings delineate the patterns of severe malaria in children in a West African mesoendemic urban setting. They validate practicable prognostic indicators of life-threatening malaria for use in the limited facilities available in African health centers and provide a frame of reference for further research addressing life-threatening malaria in this setting

    Safety and efficacy of praziquantel syrup (EpiquantelÂź) against Schistosoma haematobium and Schistosoma mansoni in preschool-aged children in Niger

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    Given the characteristic age-prevalence curve of Schistosoma infection, preventive chemotherapy with praziquantel is primarily targeted at school-aged children, whilst, in highly endemic areas, other high-risk groups might be included for regular treatment. Nevertheless, schistosomiasis can affect children well before they reach school-age, but this population group is usually excluded from preventive chemotherapy. We assessed the safety and efficacy of praziquantel syrup (Epiquantel(Âź)) in preschool-aged children in three villages of Niger. Children aged ≀72 months provided multiple urine and stool samples that were microscopically examined using standard protocols. Schistosoma-positive children were treated with praziquantel syrup at a dose of 40mg/kg after a meal of millet porridge. Children remained under medical supervision for 4h and adverse events were recorded. Additionally, a questionnaire was administrated to the mothers/guardians 24h post-treatment for further probing of adverse events. Treatment efficacy was evaluated 3 and 6 weeks post-treatment using multiple stool and urine samples. A third of the 243 treated children reported adverse events within 4h, whilst a further 6.2% reported adverse events upon probing 24h post-treatment. Abdominal pain, bloody diarrhoea and sleepiness were the most common adverse events, but these were transient and self-limiting. Praziquantel syrup showed moderate-to-high efficacy against Schistosoma haematobium with egg reduction rates of 69.4% and 71.2% 3 and 6 weeks post-treatment and cure rates of 85.7% (95% confidence interval (CI) 79.7-90.5%) and 94.9% (95% CI 90.5-97.6%), respectively. Considerably lower cure and egg reduction rates were observed against Schistosoma mansoni (e.g. cure rate at 6-week post-treatment follow-up was only 50.6% (95% CI 39.9-61.2%). Concluding, praziquantel syrup is well tolerated in preschool-aged children with moderate-to-high efficacy against S. haematobium, but considerably lower efficacy against S. mansoni in Niger. A larger study is warranted to investigate the observed differences in species-specific susceptibilities and to assess operational issues and community-effectiveness

    Epidemiology of malaria in an area of seasonal transmission in Niger and implications for the design of a seasonal malaria chemoprevention strategy

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    Background: Few data are available about malaria epidemiological situation in Niger. However, implementation of new strategies such as vaccination or seasonal treatment of a target population requires the knowledge of baseline epidemiological features of malaria. A population-based study was conducted to provide better characterization of malaria seasonal variations and population groups the most at risk in this particular area. Methods: From July 2007 to December 2009, presumptive cases of malaria among a study population living in a typical Sahelian village of Niger were recorded, and confirmed by microscopic examination. In parallel, asymptomatic carriers were actively detected at the end of each dry season in 2007, 2008 and 2009. Results: Among the 965 presumptive malaria cases recorded, 29% were confirmed by microscopic examination. The incidence of malaria was found to decrease significantly with age (p < 0.01). The mean annual incidence was 0.254. The results show that the risk of malaria was higher in children under ten years (p < 0.0001). The number of malaria episodes generally followed the temporal pattern of changes in precipitation levels, with a peak of transmission in August and September. One-thousand and ninety subjects were submitted to an active detection of asymptomatic carriage of whom 16% tested positive; asymptomatic carriage decreased with increasing age. A higher prevalence of gametocyte carriage among asymptomatic population was recorded in children aged two to ten years, though it did not reach significance. Conclusions: In Southern Niger, malaria transmission mostly occurs from July to October. Children aged two to ten years are the most at risk of malaria, and may also represent the main reservoir for gametocytes. Strategies such as intermittent preventive treatment in children (IPTc) could be of interest in this area, where malaria transmission is highly seasonal. Based on these preliminary data, a pilot study could be implemented in Zindarou using IPTc targeting children aged two to ten years, during the three months of malaria transmission, together with an accurate monitoring of drug resistance.France. Ministère des affaires étrangèresInstitut Pasteur International Networ

    Plasmodium falciparum kelch13 polymorphisms identified after treatment failure with artemisinin-based combination therapy in Niger

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    Abstract Background Artemisinin-based combination therapy (ACT) is the most effective treatment for malaria, and has significantly reduced morbimortality. Polymorphisms associated with the Plasmodium falciparum Kelch gene (Pfkelch13) have been associated with delayed parasite clearance even with ACT treatment. Methods The Pfkelch13 gene was sequenced from P. falciparum infected patients (n = 159) with uncomplicated malaria in Niger. An adequate clinical and parasitological response (ACPR) was reported in 155 patients. Four (n = 4) patients had treatment failure (TF) that were not reinfections—two of which had late parasitological failures (LPF) and two had late clinical failures (LCF). Results Thirteen single nucleotide polymorphisms (SNPs) were identified of which seven were non-synonymous (C469R, T508S, R515T, A578S, I465V, I437V, F506L,), and three were synonymous (P443P, P715P, L514L). Three SNP (C469R, F506L, P715P) were present before ACT treatment, while seven mutations (C469R, T508S, R515T, L514L, P443P, I437V, I465V) were selected by artemether/lumefantrine (AL)—five of which were non-synonymous (C469R, T508S, R515T, I437V, I465V). Artesunate/amodiaquine (ASAQ) has selected any mutation. One sample presented three cumulatively non-synonymous SNPs—C469R, T508S, R515T. Conclusions This study demonstrates intra-host selection of Pfkelch13 gene by AL. The study highlights the importance of LCF and LPF parasites in the selection of resistance to ACT. Further studies using gene editing are required to confirm the potential implication of resistance to ACT with the most common R515T and T508S mutations. It would also be important to elucidate the role of cumulative mutations
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